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            <h3 align="center"> Functional SNPs </h3>
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                    <!-- input SNPs -->
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                            <h3 class="panel-title">SNPs</h3>
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                            <textarea class="form-control" id="snp" maxlength="200" name="snp" rows="5" style="width: 100%;">
</textarea>
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                        <div class="panel-heading"><a href="#" style="cursor:hand"><span class="glyphicon glyphicon-hand-right" aria-hidden="true"></span> Example for SNPs panel</a>
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                        <div class="panel-body">
                            rs11633075<br>
                            rs12895055<br>
                            rs17711801<br>
                            rs2027349<br>
                            rs28618095<br>
                        </div>
                    </div>
                    <p><span class="snp-or" style="visibility:hidden;">or - Input one of the 3 panels</span></p>
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                        <h4 class="panel-title"><span class="glyphicon glyphicon-question-sign" aria-hidden="true"></span> Where does
                            this data come from?</h4>
                    </div>
                    <div class="panel-body">
                        <p class="note-source">
                            &nbsp;&nbsp;&nbsp;&nbsp; We downloaded allele-specific open chromatin informs functional
                            disease variants from Zhang et al. study. In the original study, Zhang et al. identified
                            thousands of genetic variants exhibiting allele-specific open chromatin (ASoC) by using
                            human induced pluripotent stem cell (iPSC)-derived neurons that model developing brains. We
                            collected this result and identified potential functional SNPs that affect chromatin
                            accessibility during neurodevelopment in bipolar disorder. More details about the data
                            analysis procedure can be found in the original publication. (Zhang et al. 2020.
                            Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants.
                            Science, 369(6503):561-565.
                            <a href='javascript:;' target='_blank'>[PMID: 32732423])</a>.<br>
                        <br>
                        <b> &nbsp;&nbsp;&nbsp;&nbsp; If you used the ‘Functional SNPs’ result in this database, please cite the relative references.</b>
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